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GCSH antibody

This Rabbit Polyclonal antibody specifically detects GCSH in WB and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7257311
$696.00
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for GCSH antibody (ABIN7257311)

Target

See all GCSH Antibodies
GCSH (Glycine Cleavage System H Protein (GCSH))

Reactivity

  • 40
  • 10
  • 10
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 38
  • 2
Rabbit

Clonality

  • 39
  • 1
Polyclonal

Conjugate

  • 14
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GCSH antibody is un-conjugated

Application

  • 31
  • 15
  • 13
  • 13
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human GCSH (NP_004474.2).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GCSH (Glycine Cleavage System H Protein (GCSH))

    Alternative Name

    GCSH

    Background

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

    Molecular Weight

    Observed_MW: 19 kDa

    Calculated_MW: 18 kDa

    Gene ID

    2653

    UniProt

    P23434
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